drugset / Trial / NCT03769194

Immunogenicity and Safety Study of a Vaccine Against Lyme Borreliosis, in Healthy Adults Aged 18 to 65 Years. Randomized, Controlled, Observer-blind Phase 2 Study.

NCT03769194 ↗

Phase 2 Completed 572 enrolled Pfizer
RandomizedParallel-groupQuadruple-blindPrevention

Summary

This is a randomized, observer-blind, placebo controlled, multicenter Phase 2 study conducted in two study phases: a run-in phase and a main study phase. The study was investigated 3 doses of a multivalent OspA (Outer Surface Protein A) based Lyme vaccine (VLA15) in healthy adults aged 18 to 65 years of age. Study participants received 3 immunizations of the vaccine at a monthly interval. The study assessed the immune response as well as the safety profile of the vaccine.

Timeline

Start
2018-12-17
Primary completion
2019-12-18
Completion
2020-10-02

Drugs

EvaluationDrugModalityDoseRoute
Comparator VLA15 Vaccine 90 ug Intramuscular
Comparator VLA15 Vaccine 135 ug Intramuscular
Comparator VLA15 Vaccine 180 ug Intramuscular

Indications